| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46846239-46846421 | Common:1; Rare:53 | ||||
| chr11:47248791-47248958 | Rare:69 | ||||
| chr11:47565496-47565660 | Common:3; Rare:34 | ||||
| chr11:47578955-47579157 | Rare:104; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:57712175-57712624 | Common:9; Rare:150 | ||||
| chr11:57741644-57741929 | Common:2; Rare:131 | ||||
| chr11:59142736-59142973 | Common:1; Rare:45 | ||||
| chr11:59668980-59669360 | Rare:129 | ||||
| chr11:60906427-60906800 | Rare:90 | ||||
| chr11:61333038-61333275 | Common:1; Rare:88 | ||||
| chr11:61361734-61361964 | Common:1; Rare:54 | ||||
| chr11:61362002-61362433 | Common:3; Rare:122; Clinvar:11; Clinvar (benign):1 | ||||
| chr11:61429905-61430169 | Common:1; Rare:117; Clinvar:3; Clinvar (benign):5 | ||||
| chr11:61792558-61792986 | Common:6; Rare:125 | ||||
| chr11:61967429-61967859 | Common:5; Rare:165; Clinvar:3 |